Use of tumor necrosis factor-alpha inhibitors during pregnancy among women who delivered live born infants.


Journal

Pharmacoepidemiology and drug safety
ISSN: 1099-1557
Titre abrégé: Pharmacoepidemiol Drug Saf
Pays: England
ID NLM: 9208369

Informations de publication

Date de publication:
03 2019
Historique:
received: 11 12 2017
revised: 21 08 2018
accepted: 10 10 2018
pubmed: 16 11 2018
medline: 11 4 2020
entrez: 16 11 2018
Statut: ppublish

Résumé

To describe the use of tumor necrosis factor-alpha inhibitors (TNFis) among pregnancies ending in a live birth and with a diagnosis of ankylosing spondylitis (AS), Crohn's disease (CD), juvenile idiopathic arthritis (JIA), psoriasis (PsO), psoriatic arthritis (PsA), rheumatoid arthritis (RA), or ulcerative colitis (UC). We identified pregnancies among women aged 15 to 54 years between 01/01/2004 and 09/30/2015 from 16 health plans participating in Sentinel. We inferred indication using ICD-9-CM codes in the 183-day period before conception. We assessed proportion of infliximab, etanercept, adalimumab, certolizumab pegol, and golimumab by calendar year, indication, and maternal age, and compared them to proportions in an age-matched, indication-matched, and date-matched non-pregnant cohort. Among 19 681 pregnancies with at least one chronic inflammatory condition, 2990 (15.2%) received a TNFi. In both pregnancies and matched non-pregnant cohort, TNFi use was highest (34.4%; 55.8%) for PsA patients and lowest (6.2%; 13.4%) for PsO patients. Etanercept was most frequently used among AS/JIA/PsA/PsO/RA patients, while infliximab was the preferred TNFi for CD/UC patients. Except for infliximab and certolizumab, TNFi use during pregnancy decreased after the first trimester. Pregnancies among older pregnant women (45-54 years) were more likely to be treated compared with the matched non-pregnant cohort. There was a preference for etanercept among pregnancies with AS/JIA/PsA/PsO/RA, despite the availability of other TNFis. Decline in TNFi use after the first trimester may be related to the desire to reduce TNFis transplacental transfer and to minimize infection risk to the fetus or baby associated with live vaccine immunizations after birth.

Identifiants

pubmed: 30430682
doi: 10.1002/pds.4695
doi:

Substances chimiques

Antibodies, Monoclonal 0
Antirheumatic Agents 0
Tumor Necrosis Factor-alpha 0
golimumab 91X1KLU43E
Infliximab B72HH48FLU
Etanercept OP401G7OJC

Types de publication

Journal Article Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

296-304

Subventions

Organisme : FDA HHS
ID : HHSF223200910006I
Pays : United States

Informations de copyright

© 2018 John Wiley & Sons, Ltd.

Auteurs

Efe Eworuke (E)

Division of Epidemiology II, Office of Pharmacovigilance and Epidemiology, Office of Surveillance and Epidemiology, Center for Drug Evaluation and Research, Food and Drug Administration, Silver Spring, MD, USA.

Genna Panucci (G)

Department of Population Medicine, Harvard Pilgrim Health Care Institute, Boston, MA, USA.

Margie Goulding (M)

Division of Epidemiology II, Office of Pharmacovigilance and Epidemiology, Office of Surveillance and Epidemiology, Center for Drug Evaluation and Research, Food and Drug Administration, Silver Spring, MD, USA.

Rosemarie Neuner (R)

Division of Pulmonary, Allergy and Rheumatology Products, Office of New Drugs, Center for Drug Evaluation and Research, Food and Drug Administration, Silver Spring, MD, USA.

Sengwee Toh (S)

Department of Population Medicine, Harvard Pilgrim Health Care Institute, Boston, MA, USA.

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Classifications MeSH